Senior Principal Scientist
Amgen
Senior Principal Scientist
Job Description
Career CategoryScientificJob DescriptionJoin Amgen’s Mission of Serving PatientsAt Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.Senior Principal ScientistWhat you will doLet’s do this. Let’s change the world! We are seeking an experienced toxicologist in the Product Stewardship group within our Environment, Health, Safety and Sustainability (EHSS) organization. This position has a broad reach and supports:• bringing new drugs to market, and• ensuring patient and staff safetyIn this role you will mature core toxicology programs to manage patient safety and EHSS risks of Amgen products, including those from drugs, manufacturing materials, primary containers, and drug-delivery device combination products, as they advance from development to commercialization, and post-approval. Primary role includes performing CMC/Quality toxicology assessments and supporting Occupational toxicology. Responsibilities include:Prepare toxicological assessments of leachable and extractables testing data as they relate to single-use manufacturing, primary drug containers, delivery devices and drug-device combination products.Support device organization with expertise on biocompatibility evaluations (ISO 10993-1) and more specifically on leachable substances (ISO 10993-17) for medical devices.Prepare and/or manage toxicology assessments of process reagents and excipients used in Amgen drug development processes and formulations.Prepare product quality toxicology assessments to support non-conformances and product complaints.Conduct or assist with patient and/or worker safety risk assessments.Classify drug candidates into Occupational Exposure Bands (OEBs) for worker safety and categorize hazards according to the Globally Harmonized Standard (GHS) for Safety Data Sheets (SDSs) and labeling to support worker safety.Derive Occupational Exposure Limits (OELs) for drug candidates and documented in product Hazard Assessment Monographs, to support worker safety.Monitor scientific developments and conduct desktop research including literature searches and critically evaluate and summarize scientific information and government regulations.Support scientific work including regulatory compliance, trade associations, and professional organizations relevant to work assignments.Coordinate Amgen EHSS contributions for influencing external scientific and regulatory activities and key initiatives such as ICH M7 (mutagenic impurities) and updates to EU GMPs (setting health-based limits for pharmaceuticals).The role is hybrid, option for remote work may be availableWhat we expect of youWe are all different, yet we all use our unique contributions to serve patients. The professional individual we seek is an individual with these qualificationsBasic Qualifications:Doctorate degree PhD OR PharmD OR MD [and relevant post-doc where applicable] and 2 years of toxicology experience ORMaster’s degree and 5 years of toxicology experience ORBachelor’s degree and 7 years of toxicology experiencePreferred Qualifications:MS or Ph.D. in toxicology, pharmacology, or related health sciencesToxicology board certification (DABT or ERT) and minimum 5 years of experience in the pharmaceutical/biotech industryExperience with the principles and practice of leachable/extractables studies, chemical characterization of packaging and device materials/components, and risk-based toxicology assessments of extractables and leachableKnowledgeable of the industry practice (e.g. PQRI, BPOG), as well as regulatory guidelines and standard (e.g. ICH, ISO) to support extractable/leachable assessmentsResearch skills with literature searches, toxicology databases, regulatory databases and computational tools. (e.g., OECD Toolbox, Toxtree, Benchmark Dose (BMD))Expert knowledge with resourceful data interpretation for derivation of toxicology-based limits (e.g. Permissible Daily Exposure values) and application of thresholds of toxicological concern (ICH M7 TTC, Cramer TTC)Prepare toxicological risk assessment reports on product quality and safetyExperience in hazard/risk assessment within pharmaceutical and/or biopharmaceutical industryWorking knowledge of biocompatibility evaluations (ISO10993-1) for medical devices and drug-device combination productsGood understanding of pharmaceutical developmentStrong scientific and technical writing skills and proficiency with EndNote or equivalentProficiency in Microsoft Office and other computer software systemsStrong team building skillsProcess driven with a strong Operational Excellence mindset and project management skillsStrong communication and presentation skills, action oriented, self-starting, program development and project managementWhat you can expect of usAs we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accountsA discretionary annual bonus program, or for field sales representatives, a sales-based incentive planStock-based long-term incentivesAward-winning time-off plansFlexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.Apply now and make a lasting impact with the Amgen team.careers.amgen.comIn any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.Application deadlineAmgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.SponsorshipSponsorship for this role is not guaranteed.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation..Salary Range168,392.65USD -227,825.35 USD
Locations
- US - California - Thousand Oaks
Skills Required
- pharmaceutical/biotech industryintermediate
- principlesintermediate
- biocompatibility evaluationsintermediate
- EndNoteintermediate
- Microsoft Officeintermediate
Required Qualifications
- Doctorate degree PhD OR PharmD OR MD [and relevant post-doc where applicable] and 2 years of toxicology experience OR (experience, 2 years)
- Master’s degree and 5 years of toxicology experience OR (experience, 5 years)
- Bachelor’s degree and 7 years of toxicology experience (experience, 7 years)
- Doctorate degree PhD OR PharmD OR MD [and relevant post-doc where applicable] and 2 years of toxicology experience OR (experience, 2 years)
- Master’s degree and 5 years of toxicology experience OR (experience, 5 years)
- Bachelor’s degree and 7 years of toxicology experience (experience, 7 years)
Preferred Qualifications
- MS or Ph.D. in toxicology, pharmacology, or related health sciences (experience)
- Toxicology board certification (DABT or ERT) and minimum 5 years of experience in the pharmaceutical/biotech industry (experience, 5 years)
- Experience with the principles and practice of leachable/extractables studies, chemical characterization of packaging and device materials/components, and risk-based toxicology assessments of extractables and leachable (experience)
- Knowledgeable of the industry practice (e.g. PQRI, BPOG), as well as regulatory guidelines and standard (e.g. ICH, ISO) to support extractable/leachable assessments (experience)
- Research skills with literature searches, toxicology databases, regulatory databases and computational tools. (e.g., OECD Toolbox, Toxtree, Benchmark Dose (BMD)) (experience)
- Expert knowledge with resourceful data interpretation for derivation of toxicology-based limits (e.g. Permissible Daily Exposure values) and application of thresholds of toxicological concern (ICH M7 TTC, Cramer TTC) (experience)
- Prepare toxicological risk assessment reports on product quality and safety (experience)
- Experience in hazard/risk assessment within pharmaceutical and/or biopharmaceutical industry (experience)
- Working knowledge of biocompatibility evaluations (ISO10993-1) for medical devices and drug-device combination products (experience)
- Good understanding of pharmaceutical development (experience)
- Strong scientific and technical writing skills and proficiency with EndNote or equivalent (experience)
- Proficiency in Microsoft Office and other computer software systems (experience)
- Strong team building skills (experience)
- Process driven with a strong Operational Excellence mindset and project management skills (experience)
- Strong communication and presentation skills, action oriented, self-starting, program development and project management (experience)
- MS or Ph.D. in toxicology, pharmacology, or related health sciences (experience)
- Toxicology board certification (DABT or ERT) and minimum 5 years of experience in the pharmaceutical/biotech industry (experience, 5 years)
- Experience with the principles and practice of leachable/extractables studies, chemical characterization of packaging and device materials/components, and risk-based toxicology assessments of extractables and leachable (experience)
- Knowledgeable of the industry practice (e.g. PQRI, BPOG), as well as regulatory guidelines and standard (e.g. ICH, ISO) to support extractable/leachable assessments (experience)
- Research skills with literature searches, toxicology databases, regulatory databases and computational tools. (e.g., OECD Toolbox, Toxtree, Benchmark Dose (BMD)) (experience)
- Expert knowledge with resourceful data interpretation for derivation of toxicology-based limits (e.g. Permissible Daily Exposure values) and application of thresholds of toxicological concern (ICH M7 TTC, Cramer TTC) (experience)
- Prepare toxicological risk assessment reports on product quality and safety (experience)
- Experience in hazard/risk assessment within pharmaceutical and/or biopharmaceutical industry (experience)
- Working knowledge of biocompatibility evaluations (ISO10993-1) for medical devices and drug-device combination products (experience)
- Good understanding of pharmaceutical development (experience)
- Strong scientific and technical writing skills and proficiency with EndNote or equivalent (experience)
- Proficiency in Microsoft Office and other computer software systems (experience)
- Strong team building skills (experience)
- Process driven with a strong Operational Excellence mindset and project management skills (experience)
- Strong communication and presentation skills, action oriented, self-starting, program development and project management (experience)
Responsibilities
- Let’s do this. Let’s change the world! We are seeking an experienced toxicologist in the Product Stewardship group within our Environment, Health, Safety and Sustainability (EHSS) organization. This position has a broad reach and supports:
- • bringing new drugs to market, and
- • ensuring patient and staff safety
- In this role you will mature core toxicology programs to manage patient safety and EHSS risks of Amgen products, including those from drugs, manufacturing materials, primary containers, and drug-delivery device combination products, as they advance from development to commercialization, and post-approval. Primary role includes performing CMC/Quality toxicology assessments and supporting Occupational toxicology. Responsibilities include:
- Prepare toxicological assessments of leachable and extractables testing data as they relate to single-use manufacturing, primary drug containers, delivery devices and drug-device combination products.
- Support device organization with expertise on biocompatibility evaluations (ISO 10993-1) and more specifically on leachable substances (ISO 10993-17) for medical devices.
- Prepare and/or manage toxicology assessments of process reagents and excipients used in Amgen drug development processes and formulations.
- Prepare product quality toxicology assessments to support non-conformances and product complaints.
- Conduct or assist with patient and/or worker safety risk assessments.
- Classify drug candidates into Occupational Exposure Bands (OEBs) for worker safety and categorize hazards according to the Globally Harmonized Standard (GHS) for Safety Data Sheets (SDSs) and labeling to support worker safety.
- Derive Occupational Exposure Limits (OELs) for drug candidates and documented in product Hazard Assessment Monographs, to support worker safety.
- Monitor scientific developments and conduct desktop research including literature searches and critically evaluate and summarize scientific information and government regulations.
- Support scientific work including regulatory compliance, trade associations, and professional organizations relevant to work assignments.
- Coordinate Amgen EHSS contributions for influencing external scientific and regulatory activities and key initiatives such as ICH M7 (mutagenic impurities) and updates to EU GMPs (setting health-based limits for pharmaceuticals).
- The role is hybrid, option for remote work may be available
- Prepare toxicological assessments of leachable and extractables testing data as they relate to single-use manufacturing, primary drug containers, delivery devices and drug-device combination products.
- Support device organization with expertise on biocompatibility evaluations (ISO 10993-1) and more specifically on leachable substances (ISO 10993-17) for medical devices.
- Prepare and/or manage toxicology assessments of process reagents and excipients used in Amgen drug development processes and formulations.
- Prepare product quality toxicology assessments to support non-conformances and product complaints.
- Conduct or assist with patient and/or worker safety risk assessments.
- Classify drug candidates into Occupational Exposure Bands (OEBs) for worker safety and categorize hazards according to the Globally Harmonized Standard (GHS) for Safety Data Sheets (SDSs) and labeling to support worker safety.
- Derive Occupational Exposure Limits (OELs) for drug candidates and documented in product Hazard Assessment Monographs, to support worker safety.
- Monitor scientific developments and conduct desktop research including literature searches and critically evaluate and summarize scientific information and government regulations.
- Support scientific work including regulatory compliance, trade associations, and professional organizations relevant to work assignments.
- Coordinate Amgen EHSS contributions for influencing external scientific and regulatory activities and key initiatives such as ICH M7 (mutagenic impurities) and updates to EU GMPs (setting health-based limits for pharmaceuticals).
- The role is hybrid, option for remote work may be available
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